Clinical Trials Study

Not Applicable

Post-Approval Study of the TREO Abdominal Stent-Graft System

Conditions: ABDOMINAL AORTIC ANEURYSM

Study #:
NCT04697784
Last Updated:
06/26/2025
Recruitment Status:
Active, not recruiting
Estimated Study Completion Date:
07/31/2027

Summary

The purpose of this study is to determine the long-term performance of the TREO Abdominal Stent-Graft as a treatment for patients with Infrarenal Abdominal Aortic Aneurysms or Aorto-iliac Aneurysms.

Age: 18 Years and older

Gender: All

Start Date: 01/20/2021

Primary Completion Date (Estimated): 07/31/2027

Study Completion Date (Estimated): 07/31/2027

Accepts Healthy Volunteers: No

Trial Purpose and Description

This is a prospective, multi-center, non-randomized, single-arm, post-market, non-interventional study of treatment with the TREO Abdominal Stent-Graft in subjects with Infrarenal Abdominal Aortic Aneurysms or Aorto-iliac Aneurysms. The study will include a minimum of 300 subjects treated with the TREO Abdominal Stent-Graft at up to 55 investigational sites in the US. The primary objective is the collection of real world safety and effectiveness outcomes of the TREO Abdominal Stent-Graft System in an all-comers population eligible for the endovascular treatment of AAA in routine clinical practice, with emphasis on subjects that experience a device stent-strut or barb fracture.

Eligibility Criteria

Age: 18 Years and older

Gender: All

Accepts Healthy Volunteers: No

Inclusion criteria:

* Willing and able to comply with all study procedures and visits.

* Written informed consent to participate in the study.

* Patient's aneurysm can be treated with the TREO Abdominal Stent-Graft System.

* Adequate data (medical records/imaging studies) available to analyze the primary endpoints for patients enrolled retrospectively.

Exclusion criteria:

• Medical, social or psychological problems that, in the opinion of the investigator, preclude patient from receiving treatment with the TREO Abdominal Stent-Graft System.

Principal Investigator

Evan Lipsitz, MD

For more information about this study, contact:

Evan Lipsitz

elipsitz@montefiore.org